Friedel Wenzel - Concepedia

Author

Friedel Wenzel

University of Basel

Also Known As

F Wenzel, F. Wenzel, FRIEDEL WENZEL, Friedel Wenzel

Publications

604

Citations

H-Index

Concepts

All Affiliations

University of Basel University Hospital of Basel University Children’s Hospital Basel Kantonsspital Aarau Boston Children's Hospital

About

Friedel Wenzel is an author at University of Basel specializing in medicine, pathology, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	314
2	Public Health	2	2	98
3	Social Sciences	1	1	60
4	Biology	1	1	20
5	Biostatistics	1	1	85

Friedel Wenzel

Publications

556

Citations

H-Index

Page 1

	Year	Citations
aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis Isabel Filges, Anjeung Kang, Vanessa Klug, Prenatal Diagnosis	2011	86
Novel Real-Time Quantitative PCR Test for Trisomy 21 Bernhard Zimmermann, Wolfgang Holzgreve, Friedel Wenzel, Clinical Chemistry Genetic TestingCytogeneticsGeneticsGenetic EpidemiologyDiagnosis	2002	85
Mosaic ring chromosome 8: Clinical and array‐CGH findings in partial trisomy 8 Isabel Filges, Benno Röthlisberger, Friedel Wenzel, American Journal of Medical Genetics Part A	2008	73
Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism Isabel Filges, Benno Röthlisberger, Ariane C. Blattner, Clinical Genetics GeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationSocial Sciences	2010	60
Genotyping fetal paternally inherited SNPs by MALDI‐TOF MS using cell‐free fetal DNA in maternal plasma: Influence of size fractionation Ying Li, Friedel Wenzel, Wolfgang Holzgreve, Electrophoresis Fetal Point MutationsMaldi‐tof MsGenetic TestingGenetic DisorderMedicine	2006	42
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype–genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome Isabel Filges, Benno Röthlisberger, Nemya Boesch, American Journal of Medical Genetics Part A Developmental AnomalyDevelopmental BiologyMendelian DisorderInterstitial Deletion 1Q42Genetic Disorder	2010	32
Somatic alterations in juvenile polyps from <scp><i>BMPR1A</i></scp> and <scp><i>SMAD</i></scp><i>4</i> mutation carriers Robert Blatter, Martina Plášilová, Friedel Wenzel, Genes Chromosomes and Cancer	2015	26
Reliable detection of Trisomy 21 using MALDI-TOF mass spectrometry Dorothy Jane Huang, Matthew R. Nelson, Bernhard Zimmermann, Genetics in Medicine CytogeneticsMedicineGenetic DisorderMass SpectrometryReliable Detection	2006	21
Morphogenesis of the micropylar apparatus in ovarian follicles of the fungus gnatBradysia tritici (syn.Sciara ocellaris) Friedel Wenzel, Herwig O. Gutzeit, Dieter Zissler Development Genes and Evolution BiologyFungus Gnatbradysia TriticiFungal Developmental BiologyDevelopmental BiologyOogenesis	1990	20
Familial 14.5 Mb interstitial deletion 13q21.1–13q21.33: Clinical and array‐CGH study of a benign phenotype in a three‐generation family Isabel Filges, Benno Röthlisberger, Christoph Noppen, American Journal of Medical Genetics Part A	2009	18

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